| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17968944-17969139 | Common:1; Rare:53 | ||||
| chr20:18137753-18137970 | Common:1; Rare:81 | ||||
| chr20:18467010-18467109 | Rare:25 | ||||
| chr20:18467137-18467444 | Common:1; Rare:64 | ||||
| chr20:18507371-18507619 | Common:1; Rare:68; Clinvar:1 | ||||
| chr20:18507847-18507961 | Common:1; Rare:34; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:18567329-18567520 | Common:2; Rare:68 | ||||
| chr20:20017215-20017399 | Rare:65 | ||||
| chr20:20038410-20038599 | Common:1; Rare:41 | ||||
| chr20:21303231-21303462 | Rare:75 | ||||
| chr20:21303731-21303851 | Rare:33 | ||||
| chr20:23049656-23049977 | Common:3; Rare:101 | ||||
| chr20:23086261-23086461 | Rare:40 | ||||
| chr20:23350499-23350886 | Common:4; Rare:117 | ||||
| chr20:23350966-23351007 | Rare:10 |